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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248238Generated: October 30, 2026

2-Mercaptoethanol → HCID 15029144, compound

https://huagongshe.com/reaction/2248238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1-(4-Bromophenyl)-2-(1H-1,2,4-triazol-1-yl)ethan-1-oneHCID 603161—
Solvent1-ButanolHCID 263—
SolventTolueneHCID 1140—
ProductHCID 15029144HCID 1502914415.3%

Reaction Steps

To a slurry of 27.8 g 1-(4-bromophenyl)-2-(1H-1,2,4-triazol-1-yl) ethanone in 350 ml dry toluene and 175 ml 1-butanol were added 15.6 g 2-mercaptoethanol and 24.7 g p-toluenesulfonic acid. The mixture was refluxed under a Dean-Stark trap for 50 hours. After cooling, a white solid was removed by filtration and the filtrate evaporated. The residue was taken up in chloroform and washed twice with 10% aqueous sodium hydroxide and once with water. The organic layer was dried, filtered and evaporated to leave a liquid residue. The 1-butanol in the residue was removed azeotropically three times with cyclohexane leaving a slurry. The solid was isolated by filtration to give 5.2 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039332
Source datasetuspto-grants-1991_08
ORD IDord-a732bb7a4d3647e2b87e418ae0485797
Source noteuspto-grants-1991_08